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Phenotypes Associated with This Genotype
Genotype
MGI:5566610
Allelic
Composition
Apctm1Tno/Apctm1Tno
Tg(Pbsn-cre)4Prb/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (158 available)
Tg(Pbsn-cre)4Prb mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mice die by 15 months of age

neoplasm
• a few mice develop unidentified tumors in the scrotal region, not obviously associated with the testes; these tumors are cystic and epithelial in origin
• all prostate lobes exhibit neoplasia with hyperplasia, multiple foci of squamous metaplasia and keratinization, and a prominent stromal reaction, including edema, inflammatory reaction and stromal hyperplasia by 7 months of age indicating adenocarcinoma
• the anterior prostate shows the most severe phenotype, followed by the dorsal-lateral and then ventral prostate
• small foci of tumor invasion into the stroma is seen but this is not common
• mice castrated at 6 weeks show regions of hyperplasia, and squamous metaplasia at 32 weeks later, but not carcinoma, indicating inhibition of tumor formation
• mice castrated after tumors still exhibit carcinoma 2 months postcastration
• mice develop prostatic epithelial hyperplasia and prostatic intraepithelial neoplasia (PIN) as early as 4.5 to 7 weeks of age

endocrine/exocrine glands
• mice develop prostatic epithelial hyperplasia as early as 4.5 to 7 weeks of age
• all prostate lobes exhibit neoplasia with hyperplasia, multiple foci of squamous metaplasia and keratinization, and a prominent stromal reaction, including edema, inflammatory reaction and stromal hyperplasia by 7 months of age indicating adenocarcinoma
• the anterior prostate shows the most severe phenotype, followed by the dorsal-lateral and then ventral prostate
• small foci of tumor invasion into the stroma is seen but this is not common
• mice castrated at 6 weeks show regions of hyperplasia, and squamous metaplasia at 32 weeks later, but not carcinoma, indicating inhibition of tumor formation
• mice castrated after tumors still exhibit carcinoma 2 months postcastration
• mice develop prostatic epithelial hyperplasia and prostatic intraepithelial neoplasia (PIN) as early as 4.5 to 7 weeks of age

reproductive system
• mice develop prostatic epithelial hyperplasia as early as 4.5 to 7 weeks of age
• all prostate lobes exhibit neoplasia with hyperplasia, multiple foci of squamous metaplasia and keratinization, and a prominent stromal reaction, including edema, inflammatory reaction and stromal hyperplasia by 7 months of age indicating adenocarcinoma
• the anterior prostate shows the most severe phenotype, followed by the dorsal-lateral and then ventral prostate
• small foci of tumor invasion into the stroma is seen but this is not common
• mice castrated at 6 weeks show regions of hyperplasia, and squamous metaplasia at 32 weeks later, but not carcinoma, indicating inhibition of tumor formation
• mice castrated after tumors still exhibit carcinoma 2 months postcastration
• mice develop prostatic epithelial hyperplasia and prostatic intraepithelial neoplasia (PIN) as early as 4.5 to 7 weeks of age


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/05/2024
MGI 6.24
The Jackson Laboratory